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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

methyl isoquinoline-7-carboxylate

COC(=O)c1ccc2c(c1)cncc2 Request for Quotation
Chemical Name: methyl isoquinoline-7-carboxylate
CAS Number: 178262-31-2
Product Number: AG0025VR(AGN-PC-03TO0Y)
Synonyms:
MDL No:
Molecular Formula: C11H9NO2
Molecular Weight: 187.1947

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl isoquinoline-7-carboxylate, a versatile chemical compound, finds its primary application in chemical synthesis as a key intermediate in the production of various pharmaceuticals and agrochemicals. Recognized for its structural flexibility and functional diversity, this compound serves as a vital building block in the synthesis of complex organic molecules with diverse biological activities. It plays a crucial role in the development of novel drug candidates, utilizing its unique reactivity to introduce specific functionalities and stereochemistries essential for drug design and discovery processes. Additionally, Methyl isoquinoline-7-carboxylate is employed in the synthesis of specialty chemicals, making it an indispensable component in the production of high-value compounds across industries. Its compatibility with a wide range of synthetic methodologies underscores its significance in advancing chemical research and enhancing the efficiency of synthetic pathways.